Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
  • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
  • A61K9/5073—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings
  • A61K9/5078—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings with drug-free core
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/08—Antiepileptics; Anticonvulsants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P3/00—Drugs for disorders of the metabolism
  • A61P3/06—Antihyperlipidemics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P3/00—Drugs for disorders of the metabolism
  • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
  • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
  • A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
  • A61K9/145—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic compounds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
  • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
  • A61K9/5005—Wall or coating material
  • A61K9/5021—Organic macromolecular compounds
  • A61K9/5036—Polysaccharides, e.g. gums, alginate; Cyclodextrin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
  • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
  • A61K9/5005—Wall or coating material
  • A61K9/5021—Organic macromolecular compounds
  • A61K9/5036—Polysaccharides, e.g. gums, alginate; Cyclodextrin
  • A61K9/5042—Cellulose; Cellulose derivatives, e.g. phthalate or acetate succinate esters of hydroxypropyl methylcellulose
  • A61K9/5047—Cellulose ethers containing no ester groups, e.g. hydroxypropyl methylcellulose

Definitions

• the present invention relates to a novel method for the preparation of granulates of active constituents, as well as the granulates as obtained.
• Such pharmacokinetic profiles involve the administration of large daily doses and/or concomitant administrations repeated throughout the day, and also a limited efficacy owing to the great variations in plasma concentration and a risk of intolerance due to those same variations. In addition, this is prejudicial to the observance of the treatment.
• An object of the present invention is to provide a method for the preparation of a novel galenic form enabling the above-mentioned disadvantages to be avoided.
• an object of the present invention is to provide a novel galenic form enabling the daily dose and the number of daily administrations to be reduced, by increasing the apparent half-life and the bioavailability of the active constituents.
• an object of the present invention is to provide a novel galenic form enabling the secondary effects to be reduced or suppressed by reducing the plasma concentrations used.
• an object of the present invention is to provide a novel galenic form enabling the comfort of the patient and the monitoring of the treatment to be improved by reducing the number of daily administrations.
• an object of the present invention is to provide a novel galenic form enabling the safety of the product to be improved by a stable galenic form.
• the present invention relates to a method for the preparation of a granulate of at least two active constituents, comprising a step of applying the active constituents by powdering to a solid particulate support, characterised in that the active constituents are not plant extracts.
• the expression “granulate” denotes a preparation composed of dry solid grains, each forming an aggregate of powder particles having sufficient solidity to allow various manipulations.
• the granulates are in the form of small grains of substantially uniform size and of irregular angular shape.
• the granulates according to the present invention have the characteristic that they have a shape which is quite regular, quasi-spherical and fairly smooth.
• the granulates are aggregates of various crystallised or amorphous powder particles.
• the granulates of the present invention are intended for oral administration and they are more particularly intended to be swallowed just as they are.
• the method of the invention therefore consists in mixing the active constituents in the form of a powder in the presence of solid particles as the support.
• the solid particles of the support used form a core on which the particles of the active constituents are deposited.
• the implementation of the method of the invention thus enables granulates having a core-skin structure to be obtained.
• the granulates of the present invention are characterised in that they have a smaller specific surface area. In addition, in appearance, they are relatively smooth and have a fairly regular shape.
• active constituents Of the active constituents, mention may be made in particular of antipaludials, antibiotics, antihypertensives, antivirals (and antiretrovirals), antiepileptics, the active constituents used in gastroenterology, the active constituents used in dermatology, anticancer agents especially of the cisplatin type or 5-flurouracil, as well as hypolipaemics.
• the core of the granulates of the invention is not composed of particles having a sugar sphere.
• the solid core of the granulates of the invention is not a sugar sphere.
• sucrose sphere denotes a spherical solid support having a homogeneous surface state.
• those supports are not advantageous because, on the one hand, they cause solubility problems (dissolution too slow) and, on the other hand, owing to their excessive regularity, they do not enable a homogeneous (granulated) final product to be obtained.
• the spherical supports tested such as, for example, the sugar spheres of saccharose and starch, have not given satisfactory results in terms of final dissolution of the form.
• For the mixture can then “cling” in the anfractuosities of the support grain during the powdering operations in successive layers and therefore contribute to the rounding of the grain.
• the supports used in the context of the present invention have the advantage of having a surface state which is not very homogeneous but which has anfractuosities in which the various active constituents will become fixed in the form of a powder. This choice is important in enabling a homogeneous final product to be obtained despite the mixture of at least two powders having different particle sizes.
• the solid core of the granulates of the invention is composed of particles having an average diameter of from 300 ⁇ m to 650 ⁇ m, preferably from 400 to 600 ⁇ m.
• the granulated mannitol support and more particularly the grade 400-500, is preferred because such a support has a sufficiently large size to enable smaller particles (less than 100 microns) to be fixed thereto.
• this granulate has the following particle size distribution: 20% of the particles have a diameter of less than 710 ⁇ m, 70% of the particles have a diameter of less than 500 ⁇ m and 25% of the particles have a diameter of less than 315 ⁇ m.
• the above-mentioned powdering step of the method for the preparation of the granulates of the invention may also comprise a step of spraying an aqueous, alcoholic or hydroalcoholic solution of a binder.
• the above-mentioned powdering step is carried out concomitantly with a step of spraying a binder in the form of a solution.
• An advantageous implementation of the method of the invention thus consists in applying the active constituents in the form of a powder to the above-mentioned particulate support (or core of the granulates) by alternating spraying sequences of the binder in the form of a solution.
• binders mention may be made of the majority of the hydrophilic excipients which give viscous solutions: gum arabic and gum tragacanth, methylcellulose and carboxymethylcellulose, gelatin, starches, maltodextrins, PEG 4000 and 6000 in alcoholic solution, polyvidone in aqueous or alcoholic solution and also saccharose, glucose or sorbitol solutions.
• the above-mentioned method also comprises, after the powdering step, a step of coating the granulate, in particular by depositing a coating agent in the form of a film on the granulate by lamination.
• This coating step thus enables the granulates obtained to be consolidated and possibly ensures that the taste of the active constituents is masked.
• the small specific surface area of the granulates of the invention thus permits, in the case of coating, a reduction in the amount of coating agent used and therefore a reduction in the dilution of the active constituents in the coated granulates.
• a preferred embodiment of the method of the invention consists in a method comprising, after the coating step, a step of mixing with a lubricant and/or a flavouring and/or a sweetener and/or a colouring.
• the above-mentioned method may also comprise, before the powdering step, a step of crushing the active constituents in the presence of a diluent.
• the method for the preparation of the granulates of the invention comprises the following steps:
• a particularly advantageous method according to the present invention is a method in which the solid particulate support is selected from the group composed of polyols, such as mannitol, sorbitol, maltitol or xylitol, lactose, dicalcium phosphate, carbonates, such as calcium, potassium, magnesium or sodium carbonate, gluconates, silicates, sugar crystals, saccharose and silica derivatives.
• polyols such as mannitol, sorbitol, maltitol or xylitol
• lactose dicalcium phosphate
• carbonates such as calcium, potassium, magnesium or sodium carbonate
• gluconates such as calcium, potassium, magnesium or sodium carbonate
• silicates such as calcium, potassium, magnesium or sodium carbonate
• sugar crystals such as sugar crystals, saccharose and silica derivatives.
• the solid particulate support does not comprise a cellulose compound.
• the solid particulate support is not a sugar sphere.
• the solid particulate support is composed of mannitol.
• the granulates so obtained are composed of a core composed of mannitol particles around which the particles of active constituents are deposited.
• the binder is selected from the group composed of polyvinylpyrrolidone (PVP or polyvidone), hydroxypropylmethylcellulose (HPMC), shellac, hydroxypropylcellulose (HPC), cellulose, polyols, alginates, polyglycolysed glycerides (Gelucire®) or macrogolglycerides, especially stearoyl macrogolglycerides, as well as mixtures thereof.
• PVP polyvinylpyrrolidone
• HPMC hydroxypropylmethylcellulose
• HPC hydroxypropylcellulose
• HPC hydroxypropylcellulose
• cellulose polyols
• alginates polyglycolysed glycerides
• Gelucire® polyglycolysed glycerides
• macrogolglycerides especially stearoyl macrogolglycerides, as well as mixtures thereof.
• polystylitol Of the polyols, mention may be made in particular of mannitol, sorbitol, maltitol or xylitol.
• the binders used in the method according to the present invention are not cellulose compounds. They are therefore preferably selected from the group composed of polyvinylpyrrolidone, shellac, polyols and alginates, polyglycolysed glycerides or macrogolglycerides, especially stearoyl macrogolglycerides, as well as mixtures thereof.
• coating agents used in the context of the method of the invention, it is preferable to use coating agents selected from the group composed of shellac, polyvinylpyrrolidone, polyethylene glycol, cellulose derivatives, such as HPMC or HPC, saccharose, alginate, methacrylic polymers and glycerides of fatty acids, or any other pharmaceutically acceptable coating polymer.
• coating agents selected from the group composed of shellac, polyvinylpyrrolidone, polyethylene glycol, cellulose derivatives, such as HPMC or HPC, saccharose, alginate, methacrylic polymers and glycerides of fatty acids, or any other pharmaceutically acceptable coating polymer.
• the present invention relates also to a method for the preparation of a granulate comprising an enteric coating, the method comprising a step of applying a coating agent composed of HPMCP (hydroxypropylmethylcellulose phthalate-hypromellose phthalate) or methacrylic polymers, especially Eudragit® L30D, or shellac.
• HPMCP hydroxypropylmethylcellulose phthalate-hypromellose phthalate
• methacrylic polymers especially Eudragit® L30D, or shellac.
• This enteric coating may enable the bioavailability of the active constituents to be increased, avoiding their degradation in an acidic environment.
• the present invention relates also to a method for the preparation of a granulate comprising a coating for prolonged release, the method comprising one or more steps of applying a coating agent composed of copolymers of methacrylates and acrylates Eudragit® RL, Eudragit® L100, shellac, derivatives of cellulose, especially ethylcellulose, and acrylic derivatives.
• a coating agent composed of copolymers of methacrylates and acrylates Eudragit® RL, Eudragit® L100, shellac, derivatives of cellulose, especially ethylcellulose, and acrylic derivatives.
• the granulates so obtained permit modified or delayed release of the active constituents (modified release granulates).
• the present invention relates also to a granulate which can be obtained in accordance with the method as defined above.
• the present invention relates also to a granulate of at least two active constituents, characterised in that it comprises a solid core on which the active constituents are supported and in that the active constituents are not plant extracts.
• the granulates of the present invention have a characteristic structure of the core-skin type, the core not being of the same nature as the active constituents forming the skin.
• these granulates have a multi-layer structure.
• the active constituents are deposited on the core and therefore form a layer (or skin) deposited around that core (or support).
• the core of the granulates may also be regarded as being a support on which the particles of the active constituents will become fixed.
• the core is composed of solid particles and the active constituents supported by the core are also in a solid form.
• the present invention is therefore based on the development of a novel multi-particle oral form.
• the original nature of the form presented here consists in a granulate for oral administration, permitting the administration of at least two active constituents other than plant extracts at sufficiently high doses to require only one or two administrations per day, the granulate of the invention being highly concentrated in active constituents.
• the granulates of the present invention have the advantage of reducing the number of daily administrations.
• the amount of active constituents per dose unit is preferably greater than or equal to 500 mg, advantageously greater than or equal to 1 g, and preferably greater than or equal to 1.5 g.
• the granulates of the present invention have the advantage of permitting a reduction, for the patient, of the number of daily administrations.
• the core of the granulates of the invention is composed of particles of a compound selected from the group composed of polyols, such as mannitol, sorbitol, maltitol or xylitol, lactose, dicalcium phosphate, carbonates, such as calcium, potassium, magnesium or sodium carbonate, gluconates, silicates, in particular magnesium aminosilicate (Neusilin®) sugar crystals or saccharose.
• polyols such as mannitol, sorbitol, maltitol or xylitol
• lactose dicalcium phosphate
• carbonates such as calcium, potassium, magnesium or sodium carbonate
• gluconates such as silicates, in particular magnesium aminosilicate (Neusilin®) sugar crystals or saccharose.
• the core of the granulates of the invention is composed of mannitol.
• the present invention therefore relates to granulates comprising particles of active constituents deposited on a core composed of mannitol particles.
• the granulates according to the present invention may also comprise a binder.
• the role of the binder is to bind the particles to each other, that is to say, to perfect the cohesion of the granulate.
• the binders provide for a good cohesion of the active constituents and the core in the granulates and for the rounding of the granulate.
• the binders like the active constituents, are deposited around the core of the granulates.
• the binders of the granulates of the invention are preferably selected from the group composed of starch, saccharose, gum arabic, polyvinylpyrrolidone (PVP or polyvidone), hydroxypropylmethylcellulose (HPMC), shellac, hydroxypropylcellulose (HPC), cellulose, polyols or alginates, polyglycolysed glycerides (Gelucire®) or macrogolglycerides, especially stearoyl macrogolglycerides, as well as mixtures thereof.
• the binders used in the granulates of the present invention are not cellulose compounds.
• the granulates of the invention are coated.
• the coated granulates are composed of grains coated with one or more layers of mixtures of various excipients.
• the preferred coated granulates according to the present invention comprise the active constituents deposited on a core composed of mannitol particles, as well as an additional layer composed of coating agent(s).
• the granulates of the invention have a multi-layer structure and are composed of a core, preferably based on mannitol, on which are deposited the active constituents and the binder, which are themselves coated with one or more layers of coating agent(s).
• the granulates of the invention are preferably coated with one or more coating agents selected from the group composed of shellac, polyvinylpyrrolidone, polyethylene glycol (PEG), cellulose derivatives, such as HPMC or HPC, saccharose, alginate and glycerides of fatty acids.
• coating agents selected from the group composed of shellac, polyvinylpyrrolidone, polyethylene glycol (PEG), cellulose derivatives, such as HPMC or HPC, saccharose, alginate and glycerides of fatty acids.
• the granulates of the invention are coated with shellac.
• the granulates of the invention may also be coated with one or more coating films to which one or more excipients, such as lubricants, colourings or sweeteners, are added.
• excipients such as lubricants, colourings or sweeteners
• the granulates of the invention may also contain one or more plasticisers, such as those conventionally used by the person skilled in the art.
• the granulates of the invention may also comprise an enteric coating for gastric protection. Such granulates are therefore gastro-resistant.
• Such a coating is obtained with coating agents composed in particular of HPMCP (hydroxypropylmethylcellulose phthalate-hypromellose phthalate) or methacrylic polymers, in particular Eudragit® L30D, or shellac.
• HPMCP hydroxypropylmethylcellulose phthalate-hypromellose phthalate
• methacrylic polymers in particular Eudragit® L30D, or shellac.
• the granulates of the invention may also comprise a coating for prolonged release.
• Such granulates permit modified or delayed release of the active constituents (modified release granulates).
• Such a coating is obtained with coating agents which are composed, in particular, of copolymers of methacrylates and acrylates Eudragit®RL, Eudragit® L100, shellac, derivatives of cellulose, especially ethylcellulose, and acrylic derivatives.
• the granulates according to the present invention may also comprise a lubricant and/or a flavouring and/or a sweetener and/or a colouring.
• lubricants flavourings, sweeteners and colourings which may be present in the granulates of the invention are especially as defined above.
• the granulates according to the present invention are characterised in that the core represents from 10 to 70%, and preferably from 25 to 55% by weight relative to the total weight of the granulate.
• a granulate according to the present invention comprises at least 20% by weight of active constituents, and especially from approximately 30% to approximately 60% by weight.
• the granulates of the invention preferably comprise less than 2% by weight of flavouring.
• the granulates of the invention preferably comprise less than 1.5% by weight of colouring.
• the granulates of the invention preferably comprise less than 2% by weight of sweetener.
• the granulates of the invention preferably comprise less than 4% by weight of lubricant.
• the constituents are weighed one by one, then the active constituents are introduced into a cubic mixer (of the CMS type).
• the quantity of diluent is weighed in its turn (mannitol 160) and introduced into the mixer.
• the mixer is then set in operation.
• the mixture obtained (A) is satisfactory after 10 minutes.
• the mixture is then introduced into a Forplex FLO mill and all of the mixture is crushed in such a way as to reduce the particle size of the whole (active constituents+diluent). This makes it possible to increase the difference in size of the particles of mannitol (support) (approximately 300 ⁇ ) and of the crushed mixture (less than 100 ⁇ and preferably 25 ⁇ ).
• the following step of the method is a step of powdering in which the equipment used is a conventional turbine.
• the mannitol which serves as support is introduced into a vessel, this latter is then set in rotation (approximately 20 rotations per minute) and the mixture A is deposited by sequential powdering on the mannitol support, alternating with phases of spraying of the binder solution (PVP/HPMC/OH/H 2 O).
• This step is carried out sequentially in order to enable the evaporation and the drying of the granulates.
• a drying phase is carried out in order to cause hot air at approximately 40° C. to circulate over the mass of granulates for approximately 14 hours.
• the product is sieved in such a way as to select the particles obtained.
• the mixture is then returned to the vessel.
• the following step is the step of coating.
• the solutions (or suspensions) containing the coating agents are placed successively in a low-pressure vessel subjected to agitation.
• the mass of granulates obtained is then placed in the vessel of a fluidised-air bed and the coating solutions are then sprayed successively in a continuous manner onto the granulates. Steps of drying/coating may also be carried out.
• An apparatus of the fluidised-air bed type (or similar technology) is preferably used for the step of coating due to its great effectiveness in terms of evaporation, which makes it possible to considerably reduce the coating times.
• Different types of coating may also be produced which each play a particular role, namely: consolidation, production of a hydrophobic layer, colouring, bitterisation, modification of the release of the active constituents.
• the additives such as sweeteners, lubricants, flavourings and colourings may be added to the granulates in a mixer.
• the last step consists in distributing the granulates into individual packages such as plastic ampoules or sachets.

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